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Towards wafer-size graphene layers by atmospheric pressure graphitization of silicon carbide

by: Konstantin V. Emtsev, Aaron Bostwick, Karsten Horn, Johannes Jobst, Gary L. Kellogg, Lothar Ley, Jessica L. McChesney, Taisuke Ohta, Sergey A. Reshanov, Jonas Rohrl, Eli Rotenberg, Andreas K. Schmid, Daniel Waldmann, Heiko B. Weber, Thomas Seyller
Nature Materials, Vol. 8, No. 3. (08 February 2009), pp. 203-207, doi:10.1038/nmat2382  Key: citeulike:4074883

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Abstract

Graphene, a single monolayer of graphite, has recently attracted considerable interest owing to its novel magneto-transport properties1, 2, 3, high carrier mobility and ballistic transport up to room temperature4. It has the potential for technological applications as a successor of silicon in the post Moore's law era5, 6, 7, as a single-molecule gas sensor8, in spintronics9, 10, 11, in quantum computing12 or as a terahertz oscillator13. For such applications, uniform ordered growth of graphene on an insulating substrate is necessary. The growth of graphene on insulating silicon carbide (SiC) surfaces by high-temperature annealing in vacuum was previously proposed to open a route for large-scale production of graphene-based devices5, 6. However, vacuum decomposition of SiC yields graphene layers with small grains (30–200 nm; refs 14–16). Here, we show that the ex situ graphitization of Si-terminated SiC(0001) in an argon atmosphere of about 1 bar produces monolayer graphene films with much larger domain sizes than previously attainable. Raman spectroscopy and Hall measurements confirm the improved quality of the films thus obtained. High electronic mobilities were found, which reach =2,000 cm 2 V-1 s-1 at T=27 K. The new growth process introduced here establishes a method for the synthesis of graphene films on a technologically viable basis.


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